Canonical Allele Identifier: PA916006116
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 234019
ClinVar RCV Id: RCV000216444 RCV003475036 RCV002516174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Pro71Ser
CA071275
NM_001276503.2:c.211C>T